1wa8
From Proteopedia
Line 1: | Line 1: | ||
- | [[Image:1wa8.gif|left|200px]] | + | [[Image:1wa8.gif|left|200px]] |
- | + | ||
- | '''SOLUTION STRUCTURE OF THE CFP-10.ESAT-6 COMPLEX. MAJOR VIRULENCE DETERMINANTS OF PATHOGENIC MYCOBACTERIA''' | + | {{Structure |
+ | |PDB= 1wa8 |SIZE=350|CAPTION= <scene name='initialview01'>1wa8</scene> | ||
+ | |SITE= | ||
+ | |LIGAND= | ||
+ | |ACTIVITY= | ||
+ | |GENE= | ||
+ | }} | ||
+ | |||
+ | '''SOLUTION STRUCTURE OF THE CFP-10.ESAT-6 COMPLEX. MAJOR VIRULENCE DETERMINANTS OF PATHOGENIC MYCOBACTERIA''' | ||
+ | |||
==Overview== | ==Overview== | ||
Line 7: | Line 16: | ||
==About this Structure== | ==About this Structure== | ||
- | 1WA8 is a [ | + | 1WA8 is a [[Protein complex]] structure of sequences from [http://en.wikipedia.org/wiki/Mycobacterium_bovis Mycobacterium bovis] and [http://en.wikipedia.org/wiki/Mycobacterium_tuberculosis Mycobacterium tuberculosis]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1WA8 OCA]. |
==Reference== | ==Reference== | ||
- | Structure and function of the complex formed by the tuberculosis virulence factors CFP-10 and ESAT-6., Renshaw PS, Lightbody KL, Veverka V, Muskett FW, Kelly G, Frenkiel TA, Gordon SV, Hewinson RG, Burke B, Norman J, Williamson RA, Carr MD, EMBO J. 2005 Jul 20;24(14):2491-8. Epub 2005 Jun 23. PMID:[http:// | + | Structure and function of the complex formed by the tuberculosis virulence factors CFP-10 and ESAT-6., Renshaw PS, Lightbody KL, Veverka V, Muskett FW, Kelly G, Frenkiel TA, Gordon SV, Hewinson RG, Burke B, Norman J, Williamson RA, Carr MD, EMBO J. 2005 Jul 20;24(14):2491-8. Epub 2005 Jun 23. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15973432 15973432] |
[[Category: Mycobacterium bovis]] | [[Category: Mycobacterium bovis]] | ||
[[Category: Mycobacterium tuberculosis]] | [[Category: Mycobacterium tuberculosis]] | ||
Line 41: | Line 50: | ||
[[Category: tuberculosis]] | [[Category: tuberculosis]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 14:54:18 2008'' |
Revision as of 12:54, 20 March 2008
| |||||||
Coordinates: | save as pdb, mmCIF, xml |
SOLUTION STRUCTURE OF THE CFP-10.ESAT-6 COMPLEX. MAJOR VIRULENCE DETERMINANTS OF PATHOGENIC MYCOBACTERIA
Overview
The secreted Mycobacterium tuberculosis complex proteins CFP-10 and ESAT-6 have recently been shown to play an essential role in tuberculosis pathogenesis. We have determined the solution structure of the tight, 1:1 complex formed by CFP-10 and ESAT-6, and employed fluorescence microscopy to demonstrate specific binding of the complex to the surface of macrophage and monocyte cells. A striking feature of the complex is the long flexible arm formed by the C-terminus of CFP-10, which was found to be essential for binding to the surface of cells. The surface features of the CFP-10.ESAT-6 complex, together with observed binding to specific host cells, strongly suggest a key signalling role for the complex, in which binding to cell surface receptors leads to modulation of host cell behaviour to the advantage of the pathogen.
About this Structure
1WA8 is a Protein complex structure of sequences from Mycobacterium bovis and Mycobacterium tuberculosis. Full crystallographic information is available from OCA.
Reference
Structure and function of the complex formed by the tuberculosis virulence factors CFP-10 and ESAT-6., Renshaw PS, Lightbody KL, Veverka V, Muskett FW, Kelly G, Frenkiel TA, Gordon SV, Hewinson RG, Burke B, Norman J, Williamson RA, Carr MD, EMBO J. 2005 Jul 20;24(14):2491-8. Epub 2005 Jun 23. PMID:15973432
Page seeded by OCA on Thu Mar 20 14:54:18 2008
Categories: Mycobacterium bovis | Mycobacterium tuberculosis | Protein complex | Burke, B. | Carr, M D. | Frenkiel, T A. | Gordon, S V. | Hewinson, R G. | Kelly, G. | Lightbody, K L. | Muskett, F W. | Norman, J. | Renshaw, P S. | TBSGC, TB Structural Genomics Consortium. | Veverka, V. | Williamson, R A. | Cfp-10 | Esat-6 | Four helix bundle | Helix-turn-helix | Mycobacteria | Nmr | Pathogenesis | Protein structure initiative | Psi | Solution structure | Tb structural genomics consortium | Tbsgc | Tuberculosis